Using chromosomal data in the phylogenetic and molecular dating framework: karyotype evolution and diversification inNierembergia(Solanaceae) influenced by historical changes in sea level

Plant Biology ◽  
2016 ◽  
Vol 18 (3) ◽  
pp. 514-526 ◽  
Author(s):  
M. C. Acosta ◽  
E. A. Moscone ◽  
A. A. Cocucci
2020 ◽  
Vol 44 (3) ◽  
pp. 255-268
Author(s):  
Esra MARTİN ◽  
Ahmet KAHRAMAN ◽  
Tuncay DİRMENCİ ◽  
Havva BOZKURT ◽  
Halil Erhan EROĞLU

2020 ◽  
Vol 72 (2) ◽  
pp. 203-209
Author(s):  
Mustafa Çelik ◽  
Yavuz Bağcı ◽  
Esra Martin ◽  
Halil Eroğlu

Chromosomal data and karyological relationships provide valuable information about karyotype evolution and speciation. For the genus Bunium, the chromosomal data are limited. In the present study, the chromosomal data of 10 taxa are provided, 6 of which are given for the first time, 2 present new chromosome numbers, and 2 agree with previous reports. Four different chromosome numbers (2n=18, 20, 22 and 40) were detected, and 2n=40 is a new number in the genus Bunium. B. brachyactis is the first polyploid species of the genus with a ploidy level of 4x. The most asymmetric karyotypes are those of B. pinnatifolium and B. sayae. Regarding karyological relationships, B. pinnatifolium forms a monophyletic group by quite different karyological features such as large chromosomes, more submedian chromosomes and the most asymmetric karyotypes. In addition, the other 5 taxa form a strong monophyletic group. B. verruculosum and B. ferulaceum are cytotaxonomically very close species, as are B. sayae and B. elegans var. elegans. The chromosome numbers of 2 Turkish species, B. nudum and B. sivasicum, remain unknown. The presented results provide important contributions to the cytotaxonomy of Bunium.


Genes ◽  
2019 ◽  
Vol 10 (4) ◽  
pp. 288 ◽  
Author(s):  
Viana ◽  
Ezaz ◽  
de Bello Cioffi ◽  
Jackson Almeida ◽  
Feldberg

Amazonian puffing snakes (Spilotes; Colubridae) are snakes widely distributed in the Neotropical region. However, chromosomal data are scarce in this group and, when available, are only limited to karyotype description using conventional staining. In this paper, we focused on the process of karyotype evolution and trends for sex chromosomes in two Amazonian Puffer Snakes (S. pulllatus and S. sulphureus). We performed an extensive karyotype characterization using conventional and molecular cytogenetic approaches. The karyotype of S. sulphureus (presented here for the first time) exhibits a 2n = 36, similar to that previously described in S. pullatus. Both species have highly differentiated ZZ/ZW sex chromosomes, where the W chromosome is highly heterochromatic in S. pullatus but euchromatic in S. sulphureus. Both W chromosomes are homologous between these species as revealed by cross-species comparative genomic hybridization, even with heterogeneous distributions of several repetitive sequences across their genomes, including on the Z and on the W chromosomes. Our study provides evidence that W chromosomes in these two species have shared ancestry.


Genome ◽  
1991 ◽  
Vol 34 (5) ◽  
pp. 714-717 ◽  
Author(s):  
Sheila M. Schmutz ◽  
Jane S. Moker

Karyotypes of three owl species previously not reported, the Burrowing Owl (Athene cunnicularia), the Hawk Owl (Surnia ulula), and the Western Screech Owl (Otus kennicotti), are presented. Comparison with other karyotypes in the literature suggests that the Burrowing Owl should be in a separate genus, as was previously the case. The Hawk Owl karyotype was found to bear considerable similarity to some Athene species, although we are not suggesting they should be placed in one genus. The karyotype of the Western Screech Owl appears to have diverged from the Otus species described previously, but these chromosomal data are not incompatible with these species sharing a common genus. A karyotype of the Long-eared Owl, which differs slightly from a previously published version, is presented. Relationships among the owls karyotyped to date are discussed on the basis of cladistic interpretations of these data.Key words: Strigiformes, phylogeny, karyotype, evolution, chromosome.


1975 ◽  
Vol 26 ◽  
pp. 395-407
Author(s):  
S. Henriksen

The first question to be answered, in seeking coordinate systems for geodynamics, is: what is geodynamics? The answer is, of course, that geodynamics is that part of geophysics which is concerned with movements of the Earth, as opposed to geostatics which is the physics of the stationary Earth. But as far as we know, there is no stationary Earth – epur sic monere. So geodynamics is actually coextensive with geophysics, and coordinate systems suitable for the one should be suitable for the other. At the present time, there are not many coordinate systems, if any, that can be identified with a static Earth. Certainly the only coordinate of aeronomic (atmospheric) interest is the height, and this is usually either as geodynamic height or as pressure. In oceanology, the most important coordinate is depth, and this, like heights in the atmosphere, is expressed as metric depth from mean sea level, as geodynamic depth, or as pressure. Only for the earth do we find “static” systems in use, ana even here there is real question as to whether the systems are dynamic or static. So it would seem that our answer to the question, of what kind, of coordinate systems are we seeking, must be that we are looking for the same systems as are used in geophysics, and these systems are dynamic in nature already – that is, their definition involvestime.


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